Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.14 (T)
Location

Chromosome 2:203868865 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61371608

This variant has 5 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Affy GenomeWideSNP_6.0, Illumina_ImmunoChip

About this variant

This variant overlaps 5 transcripts, has 3622 sample genotypes and is mentioned in 13 citations.

Variant displays